Category: Genetic Disorders / Connective Tissue Disorders
Osteogenesis Imperfecta (OI) is a genetic disorder characterized by brittle bones that break easily, often from mild trauma, due to defects in collagen production.
Estimated at 1 in 10,000 to 20,000 live births worldwide (Source: NIH Genetic and Rare Diseases Information Center).
Discover the latest clinical trials and treatments for Osteogenesis Imperfecta on JourneyForHealth.
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